STRIDE Study - A Study in Subjects With LOPD Who Are Currently Being Treated With ERT

Stopped early

Conditions studied: Late-onset Pompe Disease

In brief

The purpose of the study is to evaluate changes in key clinical outcome measures (eg, motor, respiratory, fatigue) in adult subjects with late-onset Pompe disease (LOPD) subjects receiving standard-of-care enzyme replacement therapy (ERT). Additionally, information gained may be used in the design and conduct of future studies in LOPD subjects.

Key facts

Study ID: NCT03347253
Run by: Amicus Therapeutics
People needed: 12
Starts: 2017-12-08
Expected to finish: 2018-11-30
Last updated by the study team: 2025-07-08

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subject has a diagnosis of Pompe disease based on documented deficiency of GAA activity and a documented GAA mutation.
Male and female subjects between 18 years and 75 years, inclusive and ≥ 50 kg.
Subject must be currently receiving standard-of-care ERT (alglucosidase alfa) at a dose of 20 mg/kg dose every other week.
Subject must have been on ERT for the preceding 2 years or more.
Subject must have an upright forced vital capacity (FVC) within 35 to 90% of predicted normal (NHANES III reference values), based on the higher of the screening or baseline value, if their 6 minute walk distance (6MWD) is > 200 m. Subject must have an upright FVC within 40 to 90% of predicted normal (NHANES III reference values), based on the higher of the screening or baseline value, if their 6MWD is ≤ 200 m. If FVC is between 80 and 90% of predicted normal, the subject may enter the study if the percent predicted FVC value drops by 10% predicted or more in supine position
Subject is able to walk at least 100 m in the 6MWT and the assessment is noted as valid.

You may not qualify if…

Subject has received any investigational therapy or pharmacological treatment for Pompe disease, other than alglucosidase alfa within 30 days or 5 half lives, whichever is shorter, prior to the Baseline Visit or is anticipated to do so during the course of the study
Subject is on any of the following prohibited medications within 30 days of baseline:
miglitol (eg, Glyset)
miglustat (eg, Zavesca)
acarbose (eg, Precose, Glucobay)
voglibose (eg, Volix, Vocarb, Volibo)
Subject requires use of invasive or non-invasive ventilatory support for > 6 hours a day while awake.
Subject has a medical or any other extenuating condition or circumstance that may, in the opinion of the investigator, pose an undue safety risk to the subject or compromise his/her ability to comply with protocol requirements. This includes clinical depression (as diagnosed by a psychiatrist or other mental health professional) with uncontrolled or poorly controlled symptoms.
Subject is breastfeeding, or is pregnant or planning to become pregnant within the next 2 years.
Other exclusion criteria according to the Lumizyme/Myozyme instructions for use.

Where it is running

University of California, Irvine — Irvine, California, United States
University of Florida Clinical Research Center — Gainesville, Florida, United States
Emory University — Decatur, Georgia, United States
University of Kansas Medical Center — Kansas City, Kansas, United States
Baystate Medical Center — Springfield, Massachusetts, United States
University of Minnesota Medical Center — Minneapolis, Minnesota, United States
Hackensack University Medical Center — Hackensack, New Jersey, United States
Jacobs & Levy Genomic Medicine and Research Program — Morristown, New Jersey, United States
Northwell Health — Great Neck, New York, United States
NYU Neurogenetics — New York, New York, United States
Duke University Medical Center — Durham, North Carolina, United States
Cincinnati Children's Hospital — Cincinnati, Ohio, United States
Ohio State University — Columbus, Ohio, United States
Oregon Health& Science University — Portland, Oregon, United States
Penn State Hershey Medical Center — Hershey, Pennsylvania, United States
University of Pittsburgh — Pittsburgh, Pennsylvania, United States
The University of Texas Health Science Center San Antonio — San Antonio, Texas, United States
Royal Adelaide Hospital — Adelaide, Australia
Antwerp University Hospital — Edegem, Belgium
Alberta Children's Hospital — Calgary, Alberta, Canada
McMaster University Medical Center — Hamilton, Ontario, Canada

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.